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2. Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. Issue 12 (16th August 2013)

3. Endocrine phenotype of 6q16.1–q21 deletion involving SIM1 and Prader–Willi syndrome‐like features. Issue 12 (16th August 2013)

4. Expanded cardiovascular phenotype of Myhre syndrome includes tetralogy of Fallot suggesting a role for SMAD4 in human neural crest defects. Issue 5 (13th January 2022)

5. Growth hormone deficiency in megalencephaly‐capillary malformation syndrome: An association with activating mutations in PIK3CA. Issue 1 (15th November 2019)

6. Growth Hormone Research Society perspective on the development of long-acting growth hormone preparations. Issue 6 (June 2016)

9. Safety of growth hormone replacement in survivors of cancer and intracranial and pituitary tumours: a consensus statement. Issue 6 (21st April 2022)